Canonical Allele Identifier: PA2573287427
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1522585
ClinVar RCV Id: RCV002036121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Lys1171Asn
CA2892404
NM_025132.4:c.3513A>T
CA356647283
NM_025132.4:c.3513A>C